Aica 4 Amino 5 Carbamoylimidazole
quinoline thiophene imidazole thiazole

AICA, 4-Amino-5-carbamoylimidazole

Taiy Chemical

    Specifications

    HS Code

    642252

    Chemical Formula C4H6N4O2
    Molar Mass 142.12 g/mol
    Appearance Solid
    Odor Odorless
    Melting Point 256 - 260 °C
    Solubility In Water Slightly soluble
    Pka Value ~3.5
    Density 1.60 g/cm³
    Cas Number 2315-06-8
    Role In Biochemistry Intermediate in purine biosynthesis

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    General Information
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    Frequently Asked Questions

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    What is AICA, 4 - Amino - 5 - carbamoylimidazole?
    AICA, 4-amino-5-carbamoyl imidazole, is an important chemical compound in the field of chemistry. This compound plays a key role in many biochemical processes and medical research.
    In terms of structure, it has a unique molecular structure and is composed of a specific atomic arrangement. 4-Amino and 5-carbamoyl are connected to the imidazole ring, giving it special chemical properties.
    In vivo, AICA participates in the synthesis and metabolism of purine nucleotides. In this complex biochemical reaction chain, it acts as a key intermediate and is indispensable for the formation of purine nucleotides. Many enzymatic reactions are carried out around it, and the complete structure of purine nucleotides is gradually constructed, and purine nucleotides are of great significance to life activities, such as the synthesis of DNA and RNA, all rely on them as basic raw materials.
    In the field of medical research, because of its key position in purine metabolism, scientists pay great attention to AICA. Part of the research is dedicated to exploring the development of new drugs based on AICA to regulate diseases caused by abnormal purine metabolism, such as certain types of cancer, immune diseases, etc. By precisely intervening in related biochemical reactions, the purpose of treating diseases may be achieved.
    Because of its unique chemical properties, AICA is also often an important starting material or reaction intermediate in the field of organic synthesis. Chemists have used ingenious reaction design to create more complex and functional organic molecules by leveraging their structural properties, opening up new avenues in materials science, drug discovery, and other fields.
    What are the main uses of AICA, 4 - Amino - 5 - carbamoylimidazole?
    4-Amino-5-tranexamimidazole (AICA) has important uses in the fields of medicine, chemical industry, and biological research.
    In the field of medicine, it is a key intermediate for the synthesis of purine nucleotide drugs. For example, some antiviral drugs use AICA to build a key structure, which is connected to other groups through specific reaction steps to construct a molecular structure with antiviral activity. It acts on the synthesis process of viral nucleic acid, interferes with virus replication, and has an important contribution to the fight against viral infections.
    In the chemical industry, AICA can be used as an important raw material for organic synthesis. Due to its special amino and methoyl structures, it can participate in a variety of chemical reactions and synthesize organic compounds with special properties, which are used to make functional materials, such as polymer materials with specific adsorption and catalytic properties, and contribute to the innovation and development of chemical materials.
    At the level of biological research, AICA is of great significance in the study of purine nucleotide biosynthesis pathway. It is a key intermediate product of this pathway. By studying the generation, transformation and regulation of AICA, scientists can gain in-depth insight into the mechanism of purine nucleotide synthesis, and then understand the laws of cell growth, proliferation and metabolism, providing key clues for basic biological research and the exploration of related disease mechanisms. For some diseases caused by abnormal purine metabolism, AICA-related research may reveal the root cause of disease and potential therapeutic targets.
    What are the physicochemical properties of AICA, 4 - Amino - 5 - carbamoylimidazole?
    4-Amino-5-aminoimidazole (AICA), this is an organic compound. Its physicochemical properties are quite unique.
    Looking at its properties, it may be a solid state at room temperature and pressure, but the specific appearance depends on its purity and crystallization. The value of its melting point is crucial to determine its purity and identify the compound. Different synthesis methods and purification degrees, or melting points vary.
    In terms of solubility, the solubility in water is related to the polar groups contained in the molecular structure. Both the amino group and the carbamoyl group have a certain polarity, and theoretically they may exhibit a certain solubility in water. However, due to the complexity of the overall structure of the molecule, the solubility may not be very high. In organic solvents, the dissolution performance varies depending on the polarity of the solvent. Polar organic solvents such as methanol and ethanol may have good solubility to them, while in non-polar organic solvents such as n-hexane and benzene, the solubility may be extremely low.
    In terms of stability, under general environmental conditions, if properly stored, or have certain stability. However, in case of extreme conditions such as high temperature, strong acid, and strong base, the molecular structure may be affected, triggering a chemical reaction. For example, in a strong acid environment, amino or carbamoyl groups may be protonated, thereby changing their chemical activity; under strong alkali conditions, hydrolysis reactions may be triggered, resulting in molecular structure fracture.
    The physicochemical properties of this compound are of great significance in the fields of organic synthesis and medicinal chemistry. Understanding its properties can better control the chemical reactions it participates in, providing a solid foundation for research and application in related fields.
    What is the use of AICA, 4 - Amino - 5 - carbamoylimidazole in synthesis?
    AICA, which is 4-amino-5-methoimidazole, has a crucial application in the process of synthesis.
    In the field of biochemistry, this is a key intermediary product in the biosynthesis of purine nucleotides. The synthesis of purines goes through many complex steps, and AICA connects them and provides the necessary framework for subsequent steps. Through a series of enzymatic reactions, AICA is gradually transformed into purine nucleotides, which play an indispensable role in the core processes of genetic information transmission and energy metabolism of organisms. If the synthesis or transformation of AICA is blocked, purine metabolism is disrupted, and many diseases may follow, such as gout.
    In the field of medicinal chemistry, AICA and its derivatives also have unique value. Because of its key position in the purine synthesis pathway, it can be used as a target to develop drugs. By precisely designing drug molecules to interact with enzymes involved in AICA-related reactions, or inhibit or promote their activity, purine synthesis rate is regulated. Some anti-cancer drug design concepts are based on this principle. Tumor cells proliferate rapidly and have a huge demand for purine nucleotides. Inhibiting AICA-related reactions can cut off the purine supply of tumor cells, thereby inhibiting their growth and division.
    In addition, in the field of microbial fermentation, understanding the mechanism of AICA synthesis can help to optimize fermentation conditions and improve the efficiency of microbial synthesis of specific products. By adjusting factors such as medium composition and culture environment, the synthesis path of AICA in microorganisms can be affected, and then the yield and quality of the final product can be regulated. Therefore, AICA is like a hub in all fields of synthesis, affecting the whole body, and has far-reaching significance for the development of life sciences and related industries.
    What are the production methods of AICA, 4 - Amino - 5 - carbamoylimidazole?
    AICA, that is, 4-amino-5-aminoimidazole, has various preparation methods. One of the common methods is chemical synthesis. With suitable starting materials, the structure of this compound is constructed through multi-step reaction. It usually starts with a simple compound containing nitrogen and carbon, and through condensation, substitution and other reactions, the desired amino groups, carbamoyl groups and other functional groups are introduced one after another. However, this chemical synthesis method requires fine control of the reaction conditions, such as temperature, pH, reaction time, etc. A slight difference will affect the yield and purity.
    The second is the biosynthetic pathway. AICA is generated by the catalytic action of microorganisms or enzymes. There are specific metabolic pathways in microorganisms that can convert substrates into AICA. This biosynthetic method is relatively green and environmentally friendly, and the reaction conditions are relatively mild. However, it also faces challenges, such as the screening and culture of microorganisms, the activity and stability of enzymes. It is necessary to carefully select suitable microbial strains and optimize the culture conditions to improve the efficiency of biosynthesis.
    Another semi-synthetic method combines the expertise of chemical synthesis and biosynthesis. First, the key intermediates are obtained by biosynthesis, and then chemically modified to obtain the final AICA product. This semi-synthetic method can not only take advantage of the advantages of biosynthesis, but also precisely regulate the structure by chemical synthesis, which is expected to improve the preparation efficiency and quality of AICA. All these preparation methods have their own advantages and disadvantages. In practical applications, it is necessary to choose the best one according to specific needs and conditions.